Not specified; not specified; competitive salary w...
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2+ years clinical research experience
Local regulatory submission preparation
Ethical committee and moh knowledge
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Thermo Fisher Scientific is seeking a Country Approval Specialist in Israel to manage and coordinate regulatory submissions necessary for activating clinical trial sites. The role requires attention to detail, organizational skills, and experience in clinical research, with a focus on ensuring compliance with local regulations and facilitating efficient site start-up processes.
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Job Summary
The role involves preparing and coordinating local regulatory submissions to activate investigative sites for global clinical trials.
Candidates will support rapid site start-up by ensuring alignment between submission activities and critical path timelines.
Thermo Fisher Scientific offers an award-winning learning program and a flexible working culture focused on work-life balance.
Matching Summary
Match Score: 75
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Thermo Fisher Scientific is seeking a Country Approval Specialist in Israel to manage and coordinate regulatory submissions necessary for activating clinical trial sites. The role requires attention to detail, organizational skills, and experience in clinical research, with a focus on ensuring compliance with local regulations and facilitating efficient site start-up processes.
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Salary
Not specified; Not specified; Competitive salary with extensive benefits package
Skills & Requirements
Must-have
2+ years clinical research experience
local regulatory submission preparation
Ethical Committee and MoH knowledge
Nice-to-have
strong negotiation skills
data-driven decision making
team collaboration abilities
Key Requirements
BS degree or international equivalent
2 or more years in clinical research site start up
Knowledge of regional/national country regulatory guidelines